EP3677572B1 - Production method for pyrazole-4-carboxamide derivative - Google Patents
Production method for pyrazole-4-carboxamide derivative Download PDFInfo
- Publication number
- EP3677572B1 EP3677572B1 EP18850343.7A EP18850343A EP3677572B1 EP 3677572 B1 EP3677572 B1 EP 3677572B1 EP 18850343 A EP18850343 A EP 18850343A EP 3677572 B1 EP3677572 B1 EP 3677572B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- group
- haloalkyl
- hydrogen atom
- pyrazole
- atom
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- ZVXKYWHJBYIYNI-UHFFFAOYSA-N 1h-pyrazole-4-carboxamide Chemical class NC(=O)C=1C=NNC=1 ZVXKYWHJBYIYNI-UHFFFAOYSA-N 0.000 title claims description 34
- 238000004519 manufacturing process Methods 0.000 title claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 62
- 238000006243 chemical reaction Methods 0.000 claims description 58
- 239000002904 solvent Substances 0.000 claims description 46
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 42
- 125000005843 halogen group Chemical group 0.000 claims description 32
- 150000001412 amines Chemical class 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 31
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 27
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 27
- 239000011541 reaction mixture Substances 0.000 claims description 26
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 25
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 23
- 239000012044 organic layer Substances 0.000 claims description 22
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 21
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 19
- 125000005347 halocycloalkyl group Chemical group 0.000 claims description 18
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 claims description 18
- 238000001914 filtration Methods 0.000 claims description 17
- 238000007098 aminolysis reaction Methods 0.000 claims description 16
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 15
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 15
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 15
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 15
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 15
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 15
- 125000004414 alkyl thio group Chemical group 0.000 claims description 15
- 125000004995 haloalkylthio group Chemical group 0.000 claims description 15
- 239000013077 target material Substances 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 12
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 12
- 239000010410 layer Substances 0.000 claims description 11
- 125000004434 sulfur atom Chemical group 0.000 claims description 11
- IMBBXSASDSZJSX-UHFFFAOYSA-N 4-Carboxypyrazole Chemical compound OC(=O)C=1C=NNC=1 IMBBXSASDSZJSX-UHFFFAOYSA-N 0.000 claims description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000000010 aprotic solvent Substances 0.000 claims description 9
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 150000004703 alkoxides Chemical class 0.000 claims description 7
- KOPFEFZSAMLEHK-UHFFFAOYSA-N 1h-pyrazole-5-carboxylic acid Chemical compound OC(=O)C=1C=CNN=1 KOPFEFZSAMLEHK-UHFFFAOYSA-N 0.000 claims description 6
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 6
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 5
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 125000000391 vinyl group Chemical class [H]C([*])=C([H])[H] 0.000 claims description 3
- 230000008021 deposition Effects 0.000 claims description 2
- JILPJDVXYVTZDQ-UHFFFAOYSA-N lithium methoxide Chemical compound [Li+].[O-]C JILPJDVXYVTZDQ-UHFFFAOYSA-N 0.000 claims description 2
- AZVCGYPLLBEUNV-UHFFFAOYSA-N lithium;ethanolate Chemical compound [Li+].CC[O-] AZVCGYPLLBEUNV-UHFFFAOYSA-N 0.000 claims description 2
- RPDAUEIUDPHABB-UHFFFAOYSA-N potassium ethoxide Chemical compound [K+].CC[O-] RPDAUEIUDPHABB-UHFFFAOYSA-N 0.000 claims description 2
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 claims description 2
- 239000013078 crystal Substances 0.000 description 70
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 57
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 30
- 230000015572 biosynthetic process Effects 0.000 description 24
- MRQQMVMIANXDKC-UHFFFAOYSA-N ethyl 3-(difluoromethyl)-1-methylpyrazole-4-carboxylate Chemical compound CCOC(=O)C1=CN(C)N=C1C(F)F MRQQMVMIANXDKC-UHFFFAOYSA-N 0.000 description 23
- 238000003786 synthesis reaction Methods 0.000 description 23
- 238000005406 washing Methods 0.000 description 23
- XCGBHLLWJZOLEM-UHFFFAOYSA-N 3-(difluoromethyl)-N-(7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1-methyl-1H-pyrazole-4-carboxamide Chemical compound CC1CC(C)(C)C(C(=CC=2)F)=C1C=2NC(=O)C1=CN(C)N=C1C(F)F XCGBHLLWJZOLEM-UHFFFAOYSA-N 0.000 description 20
- 238000005259 measurement Methods 0.000 description 18
- 150000001875 compounds Chemical class 0.000 description 17
- 238000001816 cooling Methods 0.000 description 17
- 239000000203 mixture Substances 0.000 description 17
- 239000000126 substance Substances 0.000 description 17
- 238000005160 1H NMR spectroscopy Methods 0.000 description 16
- 238000002844 melting Methods 0.000 description 16
- 230000008018 melting Effects 0.000 description 16
- 238000001953 recrystallisation Methods 0.000 description 16
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 16
- 238000011403 purification operation Methods 0.000 description 15
- USXBDIZEJAVICB-UHFFFAOYSA-N 7-fluoro-1,1,3-trimethyl-2,3-dihydroinden-4-amine Chemical compound NC1=CC=C(F)C2=C1C(C)CC2(C)C USXBDIZEJAVICB-UHFFFAOYSA-N 0.000 description 14
- 239000002585 base Substances 0.000 description 14
- 238000004128 high performance liquid chromatography Methods 0.000 description 12
- 238000000926 separation method Methods 0.000 description 11
- 239000012299 nitrogen atmosphere Substances 0.000 description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 150000003857 carboxamides Chemical class 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- CCCGEKHKTPTUHJ-UHFFFAOYSA-N N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC2=C1C1CCC2C1=C(Cl)Cl CCCGEKHKTPTUHJ-UHFFFAOYSA-N 0.000 description 6
- LDLMOOXUCMHBMZ-UHFFFAOYSA-N bixafen Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 LDLMOOXUCMHBMZ-UHFFFAOYSA-N 0.000 description 6
- 238000009776 industrial production Methods 0.000 description 6
- 239000002699 waste material Substances 0.000 description 6
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 5
- XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 description 5
- 239000000498 cooling water Substances 0.000 description 5
- SXSGXWCSHSVPGB-UHFFFAOYSA-N fluxapyroxad Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC(F)=C(F)C(F)=C1 SXSGXWCSHSVPGB-UHFFFAOYSA-N 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- UFFBMTHBGFGIHF-UHFFFAOYSA-N 2,6-dimethylaniline Chemical compound CC1=CC=CC(C)=C1N UFFBMTHBGFGIHF-UHFFFAOYSA-N 0.000 description 4
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000000855 fungicidal effect Effects 0.000 description 4
- 239000000417 fungicide Substances 0.000 description 4
- FTIKVBVUYPQUBF-UHFFFAOYSA-N 2-(3,4,5-trifluorophenyl)aniline Chemical compound NC1=CC=CC=C1C1=CC(F)=C(F)C(F)=C1 FTIKVBVUYPQUBF-UHFFFAOYSA-N 0.000 description 3
- QUVGVAKQHNJQNN-UHFFFAOYSA-N 2-(3,4-dichlorophenyl)-4-fluoroaniline Chemical compound NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 QUVGVAKQHNJQNN-UHFFFAOYSA-N 0.000 description 3
- HEIXUXGCYZHZDM-UHFFFAOYSA-N 2-(4-methylpentan-2-yl)thiophen-3-amine Chemical compound CC(C)CC(C)C=1SC=CC=1N HEIXUXGCYZHZDM-UHFFFAOYSA-N 0.000 description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000005737 Benzovindiflupyr Substances 0.000 description 3
- 239000005738 Bixafen Substances 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000005788 Fluxapyroxad Substances 0.000 description 3
- 239000005799 Isopyrazam Substances 0.000 description 3
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 3
- 239000005816 Penthiopyrad Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 150000001733 carboxylic acid esters Chemical class 0.000 description 3
- 239000007810 chemical reaction solvent Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- 239000002351 wastewater Substances 0.000 description 3
- SYTBZMRGLBWNTM-SNVBAGLBSA-N (R)-flurbiprofen Chemical compound FC1=CC([C@H](C(O)=O)C)=CC=C1C1=CC=CC=C1 SYTBZMRGLBWNTM-SNVBAGLBSA-N 0.000 description 2
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 description 2
- TWBPWBPGNQWFSJ-UHFFFAOYSA-N 2-phenylaniline Chemical compound NC1=CC=CC=C1C1=CC=CC=C1 TWBPWBPGNQWFSJ-UHFFFAOYSA-N 0.000 description 2
- LXMJXGIVXKBMQK-UHFFFAOYSA-N 3-(difluoromethyl)-1-methyl-N-(3-methylphenyl)pyrazole-4-carboxamide Chemical compound FC(C1=NN(C=C1C(=O)NC1=CC(=CC=C1)C)C)F LXMJXGIVXKBMQK-UHFFFAOYSA-N 0.000 description 2
- WUTUYTDBDVXQTQ-UHFFFAOYSA-N 3-(difluoromethyl)-1-methyl-n-phenylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1 WUTUYTDBDVXQTQ-UHFFFAOYSA-N 0.000 description 2
- MNTXRBRCVKLXMY-UHFFFAOYSA-N 3-(difluoromethyl)-N-(2,6-dimethylphenyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(C1=NN(C=C1C(=O)NC1=C(C=CC=C1C)C)C)F MNTXRBRCVKLXMY-UHFFFAOYSA-N 0.000 description 2
- YRJXUSQXKRTNNV-UHFFFAOYSA-N 3-(difluoromethyl)-N-(3-fluorophenyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(C1=NN(C=C1C(=O)NC1=CC(=CC=C1)F)C)F YRJXUSQXKRTNNV-UHFFFAOYSA-N 0.000 description 2
- QZVQQUVWFIZUBQ-UHFFFAOYSA-N 3-fluoroaniline Chemical compound NC1=CC=CC(F)=C1 QZVQQUVWFIZUBQ-UHFFFAOYSA-N 0.000 description 2
- VLBAAZYGJAXMBQ-UHFFFAOYSA-N 9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-amine Chemical compound NC1=CC=CC2=C1C1CCC2C1=C(Cl)Cl VLBAAZYGJAXMBQ-UHFFFAOYSA-N 0.000 description 2
- YHOQMAJZIIUYAZ-UHFFFAOYSA-N C1=CC=C(N)C2=C1C1C(C(C)C)C2CC1 Chemical compound C1=CC=C(N)C2=C1C1C(C(C)C)C2CC1 YHOQMAJZIIUYAZ-UHFFFAOYSA-N 0.000 description 2
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 238000011088 calibration curve Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 2
- ZZEXDJGNURSJOF-UHFFFAOYSA-N ethyl 1-methyl-3-(trifluoromethyl)pyrazole-4-carboxylate Chemical compound CCOC(=O)C1=CN(C)N=C1C(F)(F)F ZZEXDJGNURSJOF-UHFFFAOYSA-N 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 230000000269 nucleophilic effect Effects 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 2
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000010898 silica gel chromatography Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- XJEVHMGJSYVQBQ-UHFFFAOYSA-N 2,3-dihydro-1h-inden-1-amine Chemical group C1=CC=C2C(N)CCC2=C1 XJEVHMGJSYVQBQ-UHFFFAOYSA-N 0.000 description 1
- WKPVSKFZHNGTRJ-UHFFFAOYSA-N 2-[chloro(1,3-oxazolidin-2-yl)phosphoryl]-1,3-oxazolidine Chemical compound N1CCOC1P(=O)(Cl)C1NCCO1 WKPVSKFZHNGTRJ-UHFFFAOYSA-N 0.000 description 1
- KLDLRDSRCMJKGM-UHFFFAOYSA-N 3-[chloro-(2-oxo-1,3-oxazolidin-3-yl)phosphoryl]-1,3-oxazolidin-2-one Chemical compound C1COC(=O)N1P(=O)(Cl)N1CCOC1=O KLDLRDSRCMJKGM-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 206010007269 Carcinogenicity Diseases 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 1
- 229910001617 alkaline earth metal chloride Inorganic materials 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- -1 calcium chloride Chemical compound 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 230000007670 carcinogenicity Effects 0.000 description 1
- 231100000260 carcinogenicity Toxicity 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000012320 chlorinating reagent Substances 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000009938 salting Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000010421 standard material Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
Definitions
- the present invention relates to a method of producing a pyrazole-4-carboxamide derivative.
- Pyrazole-4-carboxamide derivatives are useful as agricultural chemicals or intermediates thereof, and so on.
- PTL 1 WO 2013/186325 A
- PTL 2 WO 2003/070705 A
- PTL 3 WO 2006/087343 A
- fluxapyroxad
- PTL 4 WO 2007/115765 A
- PTL 5 WO 2007/048556 A
- PTL 6 EP 0737682 A
- penthiopyrad have excellent effects as an agricultural fungicide and are widely used in the world for controlling crop diseases.
- the acid chloride is prepared by using a chlorinating agent, such as thionyl chloride and oxalyl chloride, and there were involved such problems that the number of steps to reach the carboxamide is long, that a reagent which is dangerous in handling for preparation of the acid chloride must be used, and that large quantities of waste acid and waste water come out after the reaction.
- a chlorinating agent such as thionyl chloride and oxalyl chloride
- Examples of the background art of the production method of a pyrazole-4-carboxamide derivative using the aminolysis reaction in the presence of a base include the following patent literatures: PTL 10 ( WO 2012/055864 A ) and PTL 11 ( WO 2012/175511 A ).
- PTL 10 ( WO 2012/055864 A ) describes that the pyrazole-4-carboxamide derivative can be produced from a pyrazole-4-carboxylic acid ester and an amine by using a bulky non-nucleophilic base, such as potassium tert-butoxide.
- a bulky non-nucleophilic base such as potassium tert-butoxide.
- the base is limited to the non-nucleophilic base, and silica gel chromatography is needed for purification of the target material, and therefore, it is hard to say that the foregoing method is an industrial production method.
- PTL 11 ( WO 2012/175511 A ) describes that the pyrazole-4-carboxamide derivative can be produced from a pyrazole-4-carboxylic acid ester and an amine by using a metal alkoxide as the base.
- a step of reducing the pressure in the system and removing the by-produced alcohol through azeotropic distillation with toluene as a solvent is needed, and from the standpoint of complicated operation and increase of waste liquids, it is hard to say that the method is advantageous as an industrial production method.
- the present invention is one solving the aforementioned problems involved in the background art and is to provide an industrial production method in which a pyrazole-4-carboxamide derivative that is useful as an agricultural fungicide can be obtained simply and in high yield and high purity as compared with the conventional method.
- the present inventors made extensive and intensive investigations regarding a method of producing a pyrazole-4-carboxamide derivative of the formula (1) through an aminolysis reaction of a pyrazole carboxylic acid ester of the formula (2) and an amine of the formula (3) in a solvent in the presence of a base according to the following reaction formula (A).
- reaction formula (A) it has been found that the reaction can be completed without removing a by-produced alcohol or phenyl, which is needed to be removed outside the system in the general aminolysis reaction, outside the system, thereby leading to accomplishment of the present invention.
- the present invention is to provide an industrial production method in which not only the pyrazole-4-carboxamide derivative represented by the formula (1) is obtained by a simple operation and in high yield and high purity, but also it is possible to reduce the quantities of waste acid and waste water.
- R, R 1 , R 2 , R 3 , and Qx in the formulae (1), (2), and (3) are respectively described later.
- a pyrazole-4-carboxamide derivative according to the present invention it is possible to obtain the pyrazole-4-carboxamide derivative which is useful as an agricultural fungicide, simply and in high yield and high purity as compared with the conventional method by a short process and a simple operation, and the production method of the present invention can be adopted as an industrial production method.
- the present invention relates to a production method of a pyrazole-4-carboxamide derivative represented by the formula (1) through an aminolysis reaction of a pyrazole-4-carboxylic acid ester of the formula (2) and an amine of the formula (3) in a solvent in the presence of a base according to the reaction formula (A) and is an invention of the production method in which on the occasion of reaction, the reaction can be completed without removing a by-produced alcohol or phenol outside the reaction system.
- the pyrazole-4-carboxamide derivative obtained by the aforementioned reaction is a compound represented by the formula (1).
- the pyrazole-4-carboxamide derivative represented by the formula (1) includes not only a single optical isomer and a diastereoisomer but also morphologies of a racemic mixture, a diastereoisomer mixture, and a partially separated mixture of such a compound, caused by the structure of the amine represented by the formula (2).
- the racemic mixture and the diastereoisomer mixture each mean a mixture of isomers thereof (racemate and diastereomer); and the partially separated mixture means a mixture remained resulting from separation of a part of isomers from isomers constituting a racemic mixture and a diastereoisomer mixture (for example, in the case of a racemate, a mixture of isomers in which as a result of separation of a part of the R-form or the S-form, a ratio of the R-form and S-form has changed from a typical value of 1/1 to a value of not 1/1).
- the compound represented by the formula (1) is one mentioned below.
- R 1 is a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, preferably a C1-C4 alkyl group, and especially preferably a methyl group.
- R 2 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, preferably a C1-C4 haloalkyl group, and especially preferably a difluoromethyl group or a trifluoromethyl group.
- R 3 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, and especially preferably a hydrogen atom.
- the pyrazole-4-carboxylic acid ester represented by the formula (2), which is one of the starting substances, is one mentioned below.
- R 1 is a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, preferably a C1-C4 alkyl group, and especially preferably a methyl group.
- R 2 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, preferably a C1-C4 haloalkyl group, and especially preferably a difluoromethyl group or a trifluoromethyl group.
- R 3 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, and especially preferably a hydrogen atom.
- R is a C1-C4 alkyl group or an optionally substituted phenyl group, preferably a C1-C4 alkyl group, and especially preferably an ethyl group.
- Qx represents any substituent (amine residue) of Q1, Q2, Q3, Q4, Q5, and Q6.
- R 4 , R 5 , and R 6 are the same as or different from each other and are each a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, or a C3-C6 halocycloalkyl group, provided that R 5 and R 6 may be bonded to each other to form a C3-C6 cycloalkyl group; and preferably a C1-C4 alkyl group.
- R 4 , R 5 , and R 6 are each a methyl group.
- V represents CH(R 7 ), N(R 8 ), an oxygen atom, or a sulfur atom; and R 7 and R 8 are each a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, or a C3-C6 halocycloalkyl group.
- R 7 is a hydrogen atom.
- Y represents a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, an SH group, a C1-C4 alkylthio group, or a C1-C4 haloalkylthio group, preferably a halogen atom, and especially preferably a fluorine atom.
- n is an integer of 0 to 3, preferably 0 or 1, and especially preferably 1.
- the substitution position of the fluorine atom is especially preferably the 7-position of the indane-amine.
- Y 1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a hydrogen atom, a C1-C6 alkyl group, or a halogen atom.
- n represents an integer of 1 to 5, and when n is 2, 3, 4, or 5, then Y 1 's may be the same as or different from each other.
- Y 1 and Z each represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a hydrogen atom or a halogen atom.
- p represents an integer of 1 to 4, and when p is 2, 3, or 4, then Y 1 's may be the same as or different from each other.
- n an integer of 1 to 5, and when n is 2, 3, 4, or 5, then Z's may be the same as or different from each other.
- R 9 , R 10 , R 11 , R 12 , R 13 , and R 14 are the same as or different from each other and each represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a hydrogen atom or a C1-C6 alkyl group.
- R 11 and R 12 may be bonded to each other to form a C3-C6 cycloalkyl group and R 13 and R 14 may be bonded to each other to form a C3-C6 cycloalkyl group.
- W represents a methylene group, a methine group substituted with a C1-C6 haloalkyl group, or a terminal end-substituted vinyl group represented by the formula (4).
- T represents a C1-C6 haloalkyl group or a halogen atom, and preferably a chlorine atom.
- Y 1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a C1-C6 alkyl group.
- n represents an integer of 1 to 3, and when m is 2 or 3, then Y 1 's may be the same as or different from each other.
- G represents an oxygen atom, a sulfur atom, or N(R 15 ), and R 15 represents a hydrogen atom or a C1-C6 alkyl group, and G is preferably a sulfur atom.
- Y 1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a C1-C6 alkyl group.
- n represents an integer of 1 to 3, and when m is 2 or 3, then Y 1 's may be the same as or different from each other.
- G represents an oxygen atom, a sulfur atom, or N(R 15 ), and R 15 represents a hydrogen atom or a C1-C6 alkyl group, and G is preferably a sulfur atom.
- Examples of the pyrazole-4-carboxamide derivative represented by the formula (1) include:
- Examples of the pyrazole-4-carboxylic acid ester represented by the formula (2) and the amine represented by the formula (3), all of which are used for the production, include compounds having a substituent corresponding to the pyrazole-4-carboxamide derivative represented by the formula (1), respectively.
- the production method of the pyrazole-4-carboxamide derivative of the present invention is a method of producing the pyrazole-4-carboxamide derivative represented by the formula (1) through an aminolysis reaction of the pyrazole-4-carboxylic acid ester represented by the formula (2) and the amine represented by the formula (3) in a solvent in the presence of a base and is characterized such that the reaction is completed without removing the by-produced alcohol or phenol outside the system.
- the amount of the pyrazole-4-carboxylic acid ester is in a range of 1.0 to 2.0 equivalents, and preferably in a range of 1.0 to 1.5 equivalents to 1.0 equivalent of the amine.
- the base to be used is preferably a metal alkoxide, and more preferably a non-bulky metal alkoxide.
- examples thereof include lithium methoxide, lithium ethoxide, sodium methoxide, sodium ethoxide, potassium methoxide, and potassium ethoxide, with sodium methoxide and sodium ethoxide being especially preferred.
- the use amount of the base is preferably in a range of 1.0 to 7.0 equivalents, more preferably in a range of 1.0 to 5.0 equivalents, still more preferably in a range of 1.0 to 3.0 equivalents, especially preferably in a range of 1.0 to 2.5 equivalents, and most preferably in a range of 1.4 to 2.5 equivalents to 1.0 equivalent of the amine represented by the formula (3).
- the use amount of the base falls within this range, the target material can be obtained in a high yield without removing the by-produced alcohol or phenol outside the system, and hence, such is preferred.
- the use amount of the base is less than 1.0 equivalent, there is a tendency that the reaction does not proceed, and the yield does not increase.
- the solvent which is used in the aminolysis reaction is preferably an aprotic solvent.
- the solvent include amide-based solvents, such as N,N-dimethylacetamide, N-methylpyrrolidone, N-ethylpyrrolidone, and N,N-dimethylformamide; sulfur-containing solvents, such as dimethyl sulfoxide; hydrocarbon-based solvents, such as benzene, toluene, and xylene; and halogen-based solvents, such as dichloromethane and dichloroethane.
- amide-based solvents such as N,N-dimethylacetamide, N-methylpyrrolidone, N-ethylpyrrolidone, and N,N-dimethylformamide
- sulfur-containing solvents such as dimethyl sulfoxide
- hydrocarbon-based solvents such as benzene, toluene, and xylene
- halogen-based solvents such as dichloromethane and
- N,N-dimethylacetamide, N-methylpyrrolidone, N-ethylpyrrolidone, N,N-dimethylformamide, and dimethyl sulfoxide are preferred, with N,N-dimethylacetamide, N-methylpyrrolidone, N,N-dimethylformamide, and dimethyl sulfoxide being especially preferred.
- the solvent which is used herein refers to a specified aprotic solvent that is the reaction solvent to be used on the occasion of performing the aminolysis reaction.
- a solvent existent in the reaction system is a mixed solvent containing other solvent than this aprotic solvent, there is no objection so far as the effects of the present invention are brought.
- the aprotic solvent to be used herein for the reaction becomes the solvent to be used on the occasion of the reaction as referred to in the present invention.
- examples of the case where other solvent is existent in such a reaction system include a case where a small amount of the solvent to be caused due to the raw material used is incorporated into the reaction system.
- the solvent which is incorporated in a small amount for example, in the case where a source material to be used as the raw material is diluted with a solvent different from the solvent on the occasion of performing the aminolysis reaction, when using this raw material, the solvent which dissolves the raw material therein, for example, toluene, or the solvent which dissolves the base to be used as a catalyst (for example, an alcohol in the metal alkoxide), is occasionally partially incorporated into the reaction solvent.
- the water content in such a reaction solvent is preferably 0.5% by mass or less, and especially preferably 0.1% by mass or less.
- these aprotic solvents may be used alone; or two or more thereof may be mixed and used as a mixed solvent, and as for a mixing ratio thereof, any arbitrary proportion is adaptable.
- the use amount of the solvent is in a range of 0.5 to 10.0 equivalents, and preferably in a range of 2.0 to 5.0 equivalents relative to the amine represented by the formula (3), and the concentration of the amine is preferably 50% by mass or less.
- the target material can be obtained in high purity and high yield.
- the reaction temperature is generally in a range of -20°C to 140°C, and preferably in a range of 20°C to 90°C.
- the reaction time is generally in a range of 1 to 10 hours, and preferably in a range of 2 to 5 hours.
- the reaction in the case where a metal alkoxide is used as the base in an excessive amount as 1.0 to 7.0 equivalents relative to the aforementioned amine, and preferably, the reaction is performed in the aforementioned aprotic solvent, the reaction can be completed even when the alcohol or phenol generated owing to the aminolysis reaction between the ester and the amine is not removed from the reaction system.
- the reason for this is not elucidated yet, it may be estimated that in the case where the carboxamide as a target material, which is formed along the progress of reaction, takes in a metal ion (e.g., a sodium ion) in the reaction system to form a metal salt, the reaction equilibrium shifts to the direction of carboxamide formation, whereby the reaction is possibly completed without causing a reverse reaction.
- a metal ion e.g., a sodium ion
- the resulting pyrazole-4-carboxamide derivative is deposited in the organic layer, whereby the target material can be given in high yield and high purity.
- the amount of water needed for deposition is about 1.0 to 7.0 in terms of a mass ratio relative to the used solvent, and it is about 10.0 to 180.0 in terms of a mass ratio on a basis of the amine.
- the pyrazole-4-carboxamide derivative can be given through a simple operation of adding water after completion of the reaction as mentioned above.
- water is added to the reaction mixture after the end of the reaction to perform washing, and the aqueous layer is separated to remove an unnecessary material from the organic layer containing the target material.
- the amount of water when performing washing is in a range of 5 to 150 equivalents, and preferably in a range of 10 to 50 equivalents on a basis of the amine represented by the formula (3).
- the washing can be, for example, performed in the following manner: water is added to the reaction mixture, stirring is performed, and the resultant is allowed to stand, thereby separating the organic layer and the aqueous layer from each other, followed by removing the aqueous layer.
- an alkali metal hydroxide such as potassium hydroxide and sodium hydroxide, or an alkaline earth metal hydroxide, such as calcium hydroxide can also be added.
- an alkali metal chloride such as potassium chloride and sodium chloride, or an alkaline earth metal chloride, such as calcium chloride
- the separation between the organic layer and the aqueous layer can also be made easy owing to a salting effect or the like.
- the target material after completion of the reaction, by adding water, the target material can be deposited and obtained; however, adoption of a method in which the addition of water is performed in two stages such that water is first added to perform washing and separate the organic layer and the aqueous layer from each other, and water is again added to the separated organic layer to deposit the target material is preferred from the standpoint that an inorganic material (mainly, the alkali metal hydroxide and the like) in the reaction mixture can be removed by water washing and that the purity of the pyrazole-4-carboxamide derivative can be increased.
- an inorganic material mainly, the alkali metal hydroxide and the like
- the purity equal to that in the case of performing the liquid separation can be achieved.
- the amount of water for rinsing is required to be about 2 to 10 times that in the case of liquid separation, so that the use amount of water somewhat increases; however, the purity and yield of the resulting pyrazole-4-carboxamide derivative do not change.
- the isolation of the target pyrazole-4-carboxamide derivative can be achieved by adding water directly to the reaction mixture after the end of the reaction; or adding water to the organic layer which has been obtained by adding water to the reaction mixture and performing washing and separation, to deposit the pyrazole-4-carboxamine derivative as a crystal, followed by performing solid-liquid separation.
- the temperature on the occasion of adding water to the reaction mixture after the end of the reaction varies with the reaction temperature, the solubility of the resulting pyrazole-4-carboxamide derivative, and the amount of the organic layer, it may be a temperature at which the target material is not decomposed. In general, the temperature is preferably in a range of about 20°C to 100°C, and more preferably in a range of about 40°C to 90°C.
- the crystal can be obtained.
- the separated crystal is rinsed, thereby washing the mother liquid attached to the crystal.
- the pyrazole-4-carboxamide derivative represented by the formula (1) in a high purity can be obtained.
- a purification process such as distillation, recrystallization, and column chromatography, is not required at all.
- R 1 , R 2 , R 3 , and Qx are the same as the contents mentioned previously.
- Table 1 Compound No. R 1 R 2 R 3 Qx Compound No, R 1 R 2 R 3 Qx 1 CH 3 CF 2 H H Q1 2 CH 3 CF 2 H H Q2 Y 1 n H V CH 2 3 3-CH 3 4 3-F R 4 ,R 5 ,R 6 CH 3 5 2,6-(CH 3 ) 2 9 CH 3 CF 2 H H Q4 Ym 7-F 6 CH 3 CF 2 H H Q3 R 9 ⁇ R 14 H W Y 1 p 10 H Z n T H Cl 7 Y 1 p 11 CH 3 CF 3 H Q5 4-F Z n 3',4'-(Cl) 2 8 Y 1 p G H S Z n 3',4',5'-(F) 3
- Table 1 Compound No. R 1 R 2 R 3 Qx Compound No, R 1 R 2 R 3 Qx 1 CH 3 CF 2 H H Q1 2 CH 3
- the structure of the target material was confirmed by means of the 1 H-NMR spectrum measurement at 500 MHz, and an area percentage measured by HPLC was used as the purity.
- Ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and ethyl 3-(trifluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate used in the Examples were prepared by the method described in WO 2006/090778 A .
- the structure of the target material was confirmed by means of the 1 H-NMR spectrum measurement at 500 MHz, and the purity was determined by preparing a calibration curve using a standard material by HPLC and adopting the absolute calibration curve method.
- the 7-fluoro-1,1,3-trimethyl-4-aminoindane to be used for the reaction was prepared by reference to EP 0654464 A or the like.
- the reaction mixture was cooled to 73.0°C, and 19.9 g of water was added to the organic layer, and cooling to 0°C was performed, whereby the target 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was deposited as a crystal.
- the deposited crystal was separated by means of filtration and washed with 50.0 g of water.
- the yield was 94.0% (on a basis of 3',4'-dichloro-5-fluorobiphenyl-2-ylamine), and the purity was 98.8% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- the 3',4',5'-trifluorobiphenyl-2-ylamine was prepared by reference to WO 2010/094736 A .
- the yield was 92.3% (on a basis of 3',4',5'-trifluorobiphenyl-2-ylamine), and the purity was 97.7% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- the yield was 92.0% (on a basis of the mixture of N-[(1RS,4SR,9RS)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl]amine and N-[(1RS,4SR,9SR)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl] amine), and the purity was 99.5% (the total sum of HPLC area percentages of the syn-form and the anti-form), and a purification operation, such as recrystallization, was not needed.
- the background art is in general concerned with the usual aminolysis reaction in which a by-produced alcohol or phenol is removed outside the reaction system through fractionation or the like, and the equilibrium is shifted toward the reaction production system, thereby completing the reaction, and it may be said that the treatment after the reaction is also usual one.
- the present invention is concerned with a technology in which the pyrazole-4-caroxamide derivative can be obtained in high yield and high purity by a simple method in which the reaction can be completed without removing the by-produced alcohol or phenol outside the system, and as for the treatment after the reaction, water is added after the end of the reaction, to deposit a crystal, and thus, it is noted that the present invention is concerned with an extremely simple and safe method.
- the production method of the present invention is useful as an industrial production method in which the pyrazole-4-carboxamide derivative that is useful as an agricultural fungicide can be obtained in high yield and high purity through a short process and a simple operation.
Description
- The present invention relates to a method of producing a pyrazole-4-carboxamide derivative.
- Pyrazole-4-carboxamide derivatives are useful as agricultural chemicals or intermediates thereof, and so on. For example, PTL 1 (
WO 2013/186325 A ) describes fluindapyr; PTL 2 (WO 2003/070705 A ) describes bixafen; PTL 3 (WO 2006/087343 A ) describes fluxapyroxad; PTL 4 (WO 2007/115765 A ) describes isopyrazam; PTL 5 (WO 2007/048556 A ) describes benzovindiflupyr; and PTL 6 (EP 0737682 A ) describes penthiopyrad. These have excellent effects as an agricultural fungicide and are widely used in the world for controlling crop diseases. - As a method which is known as the production method of a carboxamide derivative, a method of allowing an active type of the corresponding carboxylic acid, for example, an acid chloride, to react with an amine to obtain the carboxamide derivative, is described in PTL 2 (
WO 2003/070705 A ), PTL 7 (WO 2007/009717 A ), and PTL 8 (WO 2007/031323 A ). - In addition, a method of allowing a carboxylic acid and an amine to react with each other in the presence of a condensing agent, such as N,N'-dicyclohexylcarbodiimide and bis(2-oxo-3-oxazolidinyl)phosphoryl chloride, to obtain a carboxamide is described in PTL 3 (
WO 2006/087343 A ) and PTL 9 (WO 2005/123690 A ). - In the aforementioned method, it is needed that after converting the corresponding carboxylic acid ester into a carboxylic acid through hydrolysis, the acid chloride is prepared by using a chlorinating agent, such as thionyl chloride and oxalyl chloride, and there were involved such problems that the number of steps to reach the carboxamide is long, that a reagent which is dangerous in handling for preparation of the acid chloride must be used, and that large quantities of waste acid and waste water come out after the reaction.
- In addition, in the method of using a condensing agent, in addition to the fact that a hydrolysis step of the carboxylic acid ester is needed similar to the above, there were involved such problems that wastes which are difficultly separated from the target material are generated after the reaction, and that the bis(2-oxazolidinyl)phosphoryl chloride has carcinogenicity and is dangerous in handling.
- Meanwhile, in an aminolysis reaction capable of obtaining a target carboxamide by allowing a carboxylic acid ester and an amine to react directly with each other, the production process is shortened, and since the acid chlorination is not adopted, it is not needed to use a dangerous reagent, and safety in the operation becomes high. In addition to the above, it becomes possible to reduce wastes, such as waste acid and waste water. Thus, such a method may become an industrially advantageous production method.
- Examples of the background art of the production method of a pyrazole-4-carboxamide derivative using the aminolysis reaction in the presence of a base include the following patent literatures: PTL 10 (
WO 2012/055864 A ) and PTL 11 (WO 2012/175511 A ). - PTL 10 (
WO 2012/055864 A ) describes that the pyrazole-4-carboxamide derivative can be produced from a pyrazole-4-carboxylic acid ester and an amine by using a bulky non-nucleophilic base, such as potassium tert-butoxide. However, the base is limited to the non-nucleophilic base, and silica gel chromatography is needed for purification of the target material, and therefore, it is hard to say that the foregoing method is an industrial production method. - In addition, PTL 11 (
WO 2012/175511 A ) describes that the pyrazole-4-carboxamide derivative can be produced from a pyrazole-4-carboxylic acid ester and an amine by using a metal alkoxide as the base. However, for completion of the reaction, a step of reducing the pressure in the system and removing the by-produced alcohol through azeotropic distillation with toluene as a solvent is needed, and from the standpoint of complicated operation and increase of waste liquids, it is hard to say that the method is advantageous as an industrial production method. -
- PTL 1:
WO 2013/186325 A - PTL 2:
WO 2003/070705 A - PTL 3:
WO 2006/087343 A - PTL 4:
WO 2007/115765 A - PTL 5:
WO 2007/048556 A - PTL 6:
EP 0737682 A - PTL 7:
WO 2007/009717 A - PTL 8:
WO 2007/031323 A - PTL 9:
WO 2005/123690 A - PTL 10:
WO 2012/055864 A - PTL 11:
WO 2012/175511 A - The present invention is one solving the aforementioned problems involved in the background art and is to provide an industrial production method in which a pyrazole-4-carboxamide derivative that is useful as an agricultural fungicide can be obtained simply and in high yield and high purity as compared with the conventional method.
- The present inventors made extensive and intensive investigations regarding a method of producing a pyrazole-4-carboxamide derivative of the formula (1) through an aminolysis reaction of a pyrazole carboxylic acid ester of the formula (2) and an amine of the formula (3) in a solvent in the presence of a base according to the following reaction formula (A). As a result, surprisingly, it has been found that the reaction can be completed without removing a by-produced alcohol or phenyl, which is needed to be removed outside the system in the general aminolysis reaction, outside the system, thereby leading to accomplishment of the present invention. Specifically, the present invention is to provide an industrial production method in which not only the pyrazole-4-carboxamide derivative represented by the formula (1) is obtained by a simple operation and in high yield and high purity, but also it is possible to reduce the quantities of waste acid and waste water.
- R, R1, R2, R3, and Qx in the formulae (1), (2), and (3) are respectively described later.
- In accordance with the production method of a pyrazole-4-carboxamide derivative according to the present invention, it is possible to obtain the pyrazole-4-carboxamide derivative which is useful as an agricultural fungicide, simply and in high yield and high purity as compared with the conventional method by a short process and a simple operation, and the production method of the present invention can be adopted as an industrial production method.
- The invention is defined in the appended claims. Embodiments not encompassed by the claims are provided for reference purposes.
- The method of producing a pyrazole-4-carboxamide derivative according to the present invention is hereunder specifically described on a basis of the reaction formula (A).
- The present invention relates to a production method of a pyrazole-4-carboxamide derivative represented by the formula (1) through an aminolysis reaction of a pyrazole-4-carboxylic acid ester of the formula (2) and an amine of the formula (3) in a solvent in the presence of a base according to the reaction formula (A) and is an invention of the production method in which on the occasion of reaction, the reaction can be completed without removing a by-produced alcohol or phenol outside the reaction system.
- The pyrazole-4-carboxamide derivative obtained by the aforementioned reaction is a compound represented by the formula (1). In addition, the pyrazole-4-carboxamide derivative represented by the formula (1) includes not only a single optical isomer and a diastereoisomer but also morphologies of a racemic mixture, a diastereoisomer mixture, and a partially separated mixture of such a compound, caused by the structure of the amine represented by the formula (2).
- Here, the racemic mixture and the diastereoisomer mixture each mean a mixture of isomers thereof (racemate and diastereomer); and the partially separated mixture means a mixture remained resulting from separation of a part of isomers from isomers constituting a racemic mixture and a diastereoisomer mixture (for example, in the case of a racemate, a mixture of isomers in which as a result of separation of a part of the R-form or the S-form, a ratio of the R-form and S-form has changed from a typical value of 1/1 to a value of not 1/1).
-
- In the formula (1), R1 is a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, preferably a C1-C4 alkyl group, and especially preferably a methyl group.
- R2 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, preferably a C1-C4 haloalkyl group, and especially preferably a difluoromethyl group or a trifluoromethyl group.
- R3 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, and especially preferably a hydrogen atom.
- Qx that is an amine residue is one mentioned later.
-
- In the formula (2), R1 is a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, preferably a C1-C4 alkyl group, and especially preferably a methyl group.
- R2 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, preferably a C1-C4 haloalkyl group, and especially preferably a difluoromethyl group or a trifluoromethyl group.
- R3 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, and especially preferably a hydrogen atom.
- R is a C1-C4 alkyl group or an optionally substituted phenyl group, preferably a C1-C4 alkyl group, and especially preferably an ethyl group.
- The amine represented by the formula (3), which is to be allowed to react with the pyrazole-4-carboxylic acid ester represented by the formula (2) is one mentioned below.
H2N-Qx (3)
-
- In Q1, R4, R5, and R6 are the same as or different from each other and are each a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, or a C3-C6 halocycloalkyl group, provided that R5 and R6 may be bonded to each other to form a C3-C6 cycloalkyl group; and preferably a C1-C4 alkyl group. In particular, it is preferred that R4, R5, and R6 are each a methyl group.
- V represents CH(R7), N(R8), an oxygen atom, or a sulfur atom; and R7 and R8 are each a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, or a C3-C6 halocycloalkyl group. In particular, it is preferred that in CH(R7), R7 is a hydrogen atom.
- Y represents a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, an SH group, a C1-C4 alkylthio group, or a C1-C4 haloalkylthio group, preferably a halogen atom, and especially preferably a fluorine atom.
- m is an integer of 0 to 3, preferably 0 or 1, and especially preferably 1. In addition, the substitution position of the fluorine atom is especially preferably the 7-position of the indane-amine.
- In Q2, Y1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a hydrogen atom, a C1-C6 alkyl group, or a halogen atom.
- n represents an integer of 1 to 5, and when n is 2, 3, 4, or 5, then Y1's may be the same as or different from each other.
- In Q3, Y1 and Z each represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a hydrogen atom or a halogen atom.
- p represents an integer of 1 to 4, and when p is 2, 3, or 4, then Y1's may be the same as or different from each other.
- n represents an integer of 1 to 5, and when n is 2, 3, 4, or 5, then Z's may be the same as or different from each other.
- In Q4, R9, R10, R11, R12, R13, and R14 are the same as or different from each other and each represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a hydrogen atom or a C1-C6 alkyl group. In addition, R11 and R12 may be bonded to each other to form a C3-C6 cycloalkyl group and R13 and R14 may be bonded to each other to form a C3-C6 cycloalkyl group.
-
- In the formula, T represents a C1-C6 haloalkyl group or a halogen atom, and preferably a chlorine atom.
- In Q5, Y1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a C1-C6 alkyl group.
- m represents an integer of 1 to 3, and when m is 2 or 3, then Y1's may be the same as or different from each other.
- G represents an oxygen atom, a sulfur atom, or N(R15), and R15 represents a hydrogen atom or a C1-C6 alkyl group, and G is preferably a sulfur atom.
- In Q6, Y1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, and preferably a C1-C6 alkyl group.
- m represents an integer of 1 to 3, and when m is 2 or 3, then Y1's may be the same as or different from each other.
- G represents an oxygen atom, a sulfur atom, or N(R15), and R15 represents a hydrogen atom or a C1-C6 alkyl group, and G is preferably a sulfur atom.
- Examples of the pyrazole-4-carboxamide derivative represented by the formula (1) include:
- 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide: a general name: fluindapyr,
- 3-(difluoromethyl)-1-methyl-N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-pyrazole-4-carboxamide: a general name: bixafen,
- 3-(difluoromethyl)-1-methyl-N-(3',4',5'-trifluorobipenyl)-pyrazole-4-carboxamide: a general name: fluxapyroxad,
- a mixture of a syn-form: 3-(difluoromethyl)-1-methyl-N-((1RS,4SR,9RS)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl)pyrazole-4-carboxamide and an anti-form: 3-(difluoromethyl)-1-methyl-N-((1RS,4SR,9SR)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl)pyrazole-4-carboxamide: a general name: isopyrazam,
- 3-(difluoromethyl)-1-methyl-N-(9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)pyrazole-4-carboxamide: a general name: benzovindiflupyr, and
- (RS)-N-[2-(1,3-dimethylbutyl)-3-thienyl]-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide: a general name: penthiopyrad.
- Examples of the pyrazole-4-carboxylic acid ester represented by the formula (2) and the amine represented by the formula (3), all of which are used for the production, include compounds having a substituent corresponding to the pyrazole-4-carboxamide derivative represented by the formula (1), respectively.
- The production method of the pyrazole-4-carboxamide derivative of the present invention is a method of producing the pyrazole-4-carboxamide derivative represented by the formula (1) through an aminolysis reaction of the pyrazole-4-carboxylic acid ester represented by the formula (2) and the amine represented by the formula (3) in a solvent in the presence of a base and is characterized such that the reaction is completed without removing the by-produced alcohol or phenol outside the system.
- In the present invention, in the aminolysis reaction, as for a charging ratio of the pyrazole-4-carboxylic acid ester represented by the formula (2) and the amine represented by the formula (3), the amount of the pyrazole-4-carboxylic acid ester is in a range of 1.0 to 2.0 equivalents, and preferably in a range of 1.0 to 1.5 equivalents to 1.0 equivalent of the amine.
- In the present invention, in the aminolysis reaction, the base to be used is preferably a metal alkoxide, and more preferably a non-bulky metal alkoxide. Specifically, examples thereof include lithium methoxide, lithium ethoxide, sodium methoxide, sodium ethoxide, potassium methoxide, and potassium ethoxide, with sodium methoxide and sodium ethoxide being especially preferred.
- The use amount of the base is preferably in a range of 1.0 to 7.0 equivalents, more preferably in a range of 1.0 to 5.0 equivalents, still more preferably in a range of 1.0 to 3.0 equivalents, especially preferably in a range of 1.0 to 2.5 equivalents, and most preferably in a range of 1.4 to 2.5 equivalents to 1.0 equivalent of the amine represented by the formula (3). When the use amount of the base falls within this range, the target material can be obtained in a high yield without removing the by-produced alcohol or phenol outside the system, and hence, such is preferred. In the case where the use amount of the base is less than 1.0 equivalent, there is a tendency that the reaction does not proceed, and the yield does not increase.
- In the present invention, the solvent which is used in the aminolysis reaction is preferably an aprotic solvent. Specific examples of the solvent include amide-based solvents, such as N,N-dimethylacetamide, N-methylpyrrolidone, N-ethylpyrrolidone, and N,N-dimethylformamide; sulfur-containing solvents, such as dimethyl sulfoxide; hydrocarbon-based solvents, such as benzene, toluene, and xylene; and halogen-based solvents, such as dichloromethane and dichloroethane. In addition, of these aprotic solvents, N,N-dimethylacetamide, N-methylpyrrolidone, N-ethylpyrrolidone, N,N-dimethylformamide, and dimethyl sulfoxide are preferred, with N,N-dimethylacetamide, N-methylpyrrolidone, N,N-dimethylformamide, and dimethyl sulfoxide being especially preferred.
- The solvent which is used herein refers to a specified aprotic solvent that is the reaction solvent to be used on the occasion of performing the aminolysis reaction. However, in the case of using this aprotic solvent, even when a solvent existent in the reaction system is a mixed solvent containing other solvent than this aprotic solvent, there is no objection so far as the effects of the present invention are brought. The aprotic solvent to be used herein for the reaction becomes the solvent to be used on the occasion of the reaction as referred to in the present invention. In this case, examples of the case where other solvent is existent in such a reaction system include a case where a small amount of the solvent to be caused due to the raw material used is incorporated into the reaction system.
- As the solvent which is incorporated in a small amount, for example, in the case where a source material to be used as the raw material is diluted with a solvent different from the solvent on the occasion of performing the aminolysis reaction, when using this raw material, the solvent which dissolves the raw material therein, for example, toluene, or the solvent which dissolves the base to be used as a catalyst (for example, an alcohol in the metal alkoxide), is occasionally partially incorporated into the reaction solvent.
- The water content in such a reaction solvent is preferably 0.5% by mass or less, and especially preferably 0.1% by mass or less. In addition, these aprotic solvents may be used alone; or two or more thereof may be mixed and used as a mixed solvent, and as for a mixing ratio thereof, any arbitrary proportion is adaptable.
- The use amount of the solvent is in a range of 0.5 to 10.0 equivalents, and preferably in a range of 2.0 to 5.0 equivalents relative to the amine represented by the formula (3), and the concentration of the amine is preferably 50% by mass or less. In the case of performing the reaction by using the solvent under such a condition, the target material can be obtained in high purity and high yield.
- In the present invention, in the aminolysis reaction, the reaction temperature is generally in a range of -20°C to 140°C, and preferably in a range of 20°C to 90°C.
- In the present invention, in the aminolysis reaction, the reaction time is generally in a range of 1 to 10 hours, and preferably in a range of 2 to 5 hours.
- In the present invention, in the case where a metal alkoxide is used as the base in an excessive amount as 1.0 to 7.0 equivalents relative to the aforementioned amine, and preferably, the reaction is performed in the aforementioned aprotic solvent, the reaction can be completed even when the alcohol or phenol generated owing to the aminolysis reaction between the ester and the amine is not removed from the reaction system. Although, the reason for this is not elucidated yet, it may be estimated that in the case where the carboxamide as a target material, which is formed along the progress of reaction, takes in a metal ion (e.g., a sodium ion) in the reaction system to form a metal salt, the reaction equilibrium shifts to the direction of carboxamide formation, whereby the reaction is possibly completed without causing a reverse reaction. In addition, in this case, it may also be considered to be one of causes that taking-in of a metal ion by the carboxamide is promoted by an interaction with the solvent to be used for the reaction.
- As a result, by adding water to the resulting reaction mixture and performing cooling, the resulting pyrazole-4-carboxamide derivative is deposited in the organic layer, whereby the target material can be given in high yield and high purity.
- The amount of water needed for deposition is about 1.0 to 7.0 in terms of a mass ratio relative to the used solvent, and it is about 10.0 to 180.0 in terms of a mass ratio on a basis of the amine.
- In the present invention, the pyrazole-4-carboxamide derivative can be given through a simple operation of adding water after completion of the reaction as mentioned above. However, prior to this, it is preferred that before depositing the pyrazole-4-carboxamide derivative by the addition of water to the reaction mixture after the end of the reaction, water is added to the reaction mixture after the end of the reaction to perform washing, and the aqueous layer is separated to remove an unnecessary material from the organic layer containing the target material. The amount of water when performing washing is in a range of 5 to 150 equivalents, and preferably in a range of 10 to 50 equivalents on a basis of the amine represented by the formula (3). The washing can be, for example, performed in the following manner: water is added to the reaction mixture, stirring is performed, and the resultant is allowed to stand, thereby separating the organic layer and the aqueous layer from each other, followed by removing the aqueous layer.
- On the occasion of separating the organic layer and the aqueous layer from each other, in order to enhance the separation state, an alkali metal hydroxide, such as potassium hydroxide and sodium hydroxide, or an alkaline earth metal hydroxide, such as calcium hydroxide can also be added. In addition, by adding an alkali metal chloride, such as potassium chloride and sodium chloride, or an alkaline earth metal chloride, such as calcium chloride, the separation between the organic layer and the aqueous layer can also be made easy owing to a salting effect or the like.
- In summary, in the present invention, after completion of the reaction, by adding water, the target material can be deposited and obtained; however, adoption of a method in which the addition of water is performed in two stages such that water is first added to perform washing and separate the organic layer and the aqueous layer from each other, and water is again added to the separated organic layer to deposit the target material is preferred from the standpoint that an inorganic material (mainly, the alkali metal hydroxide and the like) in the reaction mixture can be removed by water washing and that the purity of the pyrazole-4-carboxamide derivative can be increased.
- However, even in the case where the liquid separation between the organic layer and the aqueous layer as mentioned above is not performed, when a crystal of the pyrazole-4-caroxamide derivative which has been deposited by the addition of water is rinsed with water, the purity equal to that in the case of performing the liquid separation can be achieved. In this case, the amount of water for rinsing is required to be about 2 to 10 times that in the case of liquid separation, so that the use amount of water somewhat increases; however, the purity and yield of the resulting pyrazole-4-carboxamide derivative do not change.
- As mentioned above, the isolation of the target pyrazole-4-carboxamide derivative can be achieved by adding water directly to the reaction mixture after the end of the reaction; or adding water to the organic layer which has been obtained by adding water to the reaction mixture and performing washing and separation, to deposit the pyrazole-4-carboxamine derivative as a crystal, followed by performing solid-liquid separation. In addition, though the temperature on the occasion of adding water to the reaction mixture after the end of the reaction varies with the reaction temperature, the solubility of the resulting pyrazole-4-carboxamide derivative, and the amount of the organic layer, it may be a temperature at which the target material is not decomposed. In general, the temperature is preferably in a range of about 20°C to 100°C, and more preferably in a range of about 40°C to 90°C.
- Subsequently, by performing cooling, the crystal can be obtained. On this occasion, regardless of whether or not performing the washing and separation, in all of the methods, it is preferred that the separated crystal is rinsed, thereby washing the mother liquid attached to the crystal.
- By drying the resulting crystal, the pyrazole-4-carboxamide derivative represented by the formula (1) in a high purity can be obtained. On this occasion, a purification process, such as distillation, recrystallization, and column chromatography, is not required at all.
- The present invention is hereunder described in detail on a basis of Examples, but it should be construed that the present invention is not limited by these Examples.
-
- In the formula, R1, R2, R3, and Qx are the same as the contents mentioned previously.
Table 1 Compound No. R1 R2 R3 Qx Compound No, R1 R2 R3 Qx 1 CH3 CF2H H Q1 2 CH3 CF2H H Q2 Y1n H V CH2 3 3-CH3 4 3-F R4,R5,R6 CH3 5 2,6-(CH3)2 9 CH3 CF2H H Q4 Ym 7-F 6 CH3 CF2H H Q3 R9∼R14 H W Y1 p 10 H Zn T H Cl 7 Y1 p 11 CH3 CF3 H Q5 4-F Zn 3',4'-(Cl)2 8 Y1 p G H S Zn 3',4',5'-(F)3 - The structure of the target material was confirmed by means of the 1H-NMR spectrum measurement at 500 MHz, and an area percentage measured by HPLC was used as the purity.
- Ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and ethyl 3-(trifluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate used in the Examples were prepared by the method described in
WO 2006/090778 A . - With respect to the amine, those which are commercially available were purchased and used, whereas those which are not commercially available were prepared following the reference literatures and used. The reference literatures regarding the amine preparation method are described in the following Examples.
- The structure of the target material was confirmed by means of the 1H-NMR spectrum measurement at 500 MHz, and the purity was determined by preparing a calibration curve using a standard material by HPLC and adopting the absolute calibration curve method.
- Synthesis of 3-difluoromethyl- N- (7 -fluoro -1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide (Compound No. 1: a general name: fluindapyr) Synthesis Example 1-1
- To 33.9 mL of N-methylpyrrolidone in a 200-mL four-necked flask, 79.8 g (82.6 mmol) of a 21.1% by mass toluene solution of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 64.9 g (70.4 mmol) of a 21.0% by mass toluene solution of 7-fluoro-1,1,3-trimethyl-4-aminoindane were added.
- The 7-fluoro-1,1,3-trimethyl-4-aminoindane to be used for the reaction was prepared by reference to
EP 0654464 A or the like. - Subsequently, the contents were subjected to vacuum concentration to recover 105.8 g of toluene, thereby obtaining a N-methylpyrrolidone solution of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 7-fluoro-1,1,3-trimethyl-4-aminoindane in which 6.8% mass of toluene remained. Subsequently, 10.49 g (154.2 mmol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 83.6°C for 1.5 hours. The reaction mixture was cooled to 70°C, and then, 34.3 g of water was added to wash the organic layer. After separating the aqueous layer, 104.61 g of water was added to the organic layer, and cooling to 10°C was performed, whereby the target 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was deposited as a crystal. The deposited crystal was separated by means of filtration and washed with 12.3 g of water.
- The crystal after washing was dried. As a result, 24.4 g (66.7 mmol) of 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was obtained as a white crystal. The yield was 94.5%, and the purity was 96.0%, and a purification operation, such as recrystallization, was not needed. Melting point: 170.8°C
1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane) - δ value (ppm): 1.43 (3H,d), 1.38 (3H,s), 1.44 (3H,s), 1.66 (1H,dd), 2.21 (1H,dd), 3.38 (1H,m), 3.93 (3H,s), 6.81 (1s,bs), 6.95 (1H,t), 6.70 (1H,m), 7.81 (1H,bs), 8.03 (1H,bs)
- To 8.65 mL of N-methylpyrrolidone in a 100-mL four-necked flask, 31.84 g (32.9 mmol) of a 21.1% by mass toluene solution of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 51.74 g (30.0 mmol) of a 11.2% by mass toluene solution of 7-fluoro-1,1,3-trimethyl-4-aminoindane were added.
- The contents were subjected to vacuum concentration to recover 59.4 g of toluene, thereby obtaining a N-methylpyrrolidone solution of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 7-fluoro-1,1,3-trimethyl-4-aminoindane in which 13.3% mass of toluene remained. Subsequently, 2.97 g (43.6 mmol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 75.2°C for 6.0 hours. The reaction mixture was cooled to 73.0°C, and 19.9 g of water was added to the organic layer, and cooling to 0°C was performed, whereby the target 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was deposited as a crystal. The deposited crystal was separated by means of filtration and washed with 50.0 g of water.
- The crystal after washing was dried. As a result, 9.64 g (26.4 mmol) of 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was obtained as a white crystal. The yield was 88.1%, and the purity was 96.3%, and a purification operation, such as recrystallization, was not needed. Melting point: 170.8°C
1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane) - δ value (ppm): 1.43 (3H,d), 1.38 (3H,s), 1.44 (3H,s), 1.66 (1H,dd), 2.21 (1H,dd), 3.38 (1H,m), 3.93 (3H,s), 6.81 (1s,bs), 6.95 (1H,t), 6.70 (1H,m), 7.81 (1H,bs), 8.03 (1H,bs)
- First of all, from the toluene solution of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate which was used as the starting raw material in Synthesis Example 1-1, the toluene was removed with an evaporator, to obtain ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate. The toluene was not substantially contained in the resulting concentrate, and the toluene content was almost 0%. From the toluene solution of 7-fluoro-1,1,3-trimethyl-4-aminoindane, the toluene was removed in a similar manner, to obtain 7-fluoro-1,1,3-trimethyl-4-aminoindane. The toluene was not substantially contained in the resulting concentrate, and the toluene content was almost 0%.
- Subsequently, using the thus obtained ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 7-fluoro -1,1,3-trimethyl-4-aminoindane, synthesis of 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was performed in the following manner.
- To 43.0 mL of N-methylpyrrolidone in a 200-mL four-necked flask equipped with a cooling water refluxing tube, 20.2 g (98.9 mmol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 17.4 g (90.0 mmol) of 7-fluoro-1,1,3-trimethyl-4-aminoindane were added.
- The contents were stirred to form a solution, to which was then added 13.5 g (198.2 mmol) of sodium ethoxide, followed by stirring at an internal temperature of 48.9°C for 5.5 hours. The reaction mixture was cooled to 45°C, and then, 44.7 g of water was added to wash the organic layer. After separating the aqueous layer, 73.7 g of water was added to the organic layer, and cooling to 10°C was performed, whereby the target 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was deposited as a crystal. The deposited crystal was separated by means of filtration and washed with 15.8 g of water.
- The crystal after washing was dried. As a result, 30.6 g (83.8 mmol) of 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was obtained as a white crystal. The yield was 93.0%, and the purity was 96.2%, and a purification operation, such as recrystallization, was not needed. Melting point: 170.8°C
1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane) - δ value (ppm): 1.43 (3H,d), 1.38 (3H,s), 1.44 (3H,s), 1.66 (1H,dd), 2.21 (1H,dd), 3.38 (1H,m), 3.93 (3H,s), 6.81 (1s,bs), 6.95 (1H,t), 6.70 (1H,m), 7.81 (1H,bs), 8.03 (1H,bs)
- Using the ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 7-fluoro-1,1,3-trimethyl-4-aminoindane as prepared in Synthesis Example 1-3, synthesis of 3-difluoromethyl- N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was performed in the following manner.
- To 14.1 mL of N,N-dimethylacetamide in a 100-mL four-necked flask equipped with a cooling water refluxing tube, 6.86 g (33.3 mmol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 5.80 g (30.0 mmol) of 7-fluoro-1,1,3-trimethyl-4-aminoindane were added.
- The contents were stirred to form a solution, to which was then added 4.6 g (67.6 mmol) of sodium ethoxide, followed by stirring at an internal temperature of 85°C for 1.0 hour.
- To the resulting reaction mixture, 32.0 g of water was added, and cooling to 8°C was performed, whereby the target 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was deposited as a crystal. The deposited crystal was separated by means of filtration and washed with 25.0 g of water.
- The crystal after washing was dried. As a result, 9.9 g (27.4 mmol) of 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was obtained as a white crystal. The yield was 91.4%, and the purity was 97.3%, and a purification operation, such as recrystallization, was not needed. Melting point: 170.8°C
1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane) - δ value (ppm): 1.43 (3H,d), 1.38 (3H,s), 1.44 (3H,s), 1.66 (1H,dd), 2.21 (1H,dd), 3.38 (1H,m), 3.93 (3H,s), 6.81 (1s,bs), 6.95 (1H,t), 6.70 (1H,m), 7.81 (1H,bs), 8.03 (1H,bs)
- Using the ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 7-fluoro-1,1,3-trimethyl-4-aminoindane as prepared in Synthesis Example 1-3, synthesis of 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was performed in the following manner.
- To 10.7 mL of dimethyl sulfoxide in a 100-mL four-necked flask equipped with a cooling water refluxing tube, 6.7 g (32.8 mmol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 5.8 g (30.0 mmol) of 7-fluoro-1,1,3-trimethyl-4-aminoindane were added.
- The contents were stirred to form a solution, to which was then added 4.6 g (67.6 mmol) of sodium ethoxide, followed by stirring at an internal temperature of 84°C for 1.0 hour.
- To the resulting reaction mixture, 32.8 g of water was added, and cooling to 10°C was performed, whereby the target 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was deposited as a crystal. The deposited crystal was separated by means of filtration and washed with 50.0 g of water.
- The crystal after washing was dried. As a result, 10.3 g (28.2 mmol) of 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide was obtained as a white crystal. The yield was 94.1%, and the purity was 96.3%, and a purification operation, such as recrystallization, was not needed. Melting point: 170.8°C
1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane) - δ value (ppm): 1.43 (3H,d), 1.38 (3H,s), 1.44 (3H,s), 1.66 (1H,dd), 2.21 (1H,dd), 3.38 (1H,m), 3.93 (3H,s), 6.81 (1s,bs), 6.95 (1H,t), 6.70 (1H,m), 7.81 (1H,bs), 8.03 (1H,bs)
- As an example of the conventional method, an example of performing the synthesis according to the method described in PTL 10 (
WO 2012/055864 A ) is shown as Reference Example 1-1. - Preparation of 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide
- To 48.8 mL of tetrahydrofuran in a 100-mL four-necked flask equipped with a cooling water refluxing tube, 6.2 g (30.3 mmol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 5.8 g (30.0 mmol) of 7-fluoro-1,1,3-trimethyl-4-aminoindane were added.
- The contents were stirred to form a solution, and subsequently, a suspension liquid having added 5.2 g (45.0 mmol) of tert-butoxypotassium and 73.0 mL of tetrahydrofuran added in a 200-mL four-necked flask equipped with a cooling water refluxing tube was dropped, followed by stirring at an internal temperature of 25°C for 5.0 hours.
- To the reaction mixture, 50.5 g of water and 156.8 g of ethyl acetate were added, and the organic layer was extracted twice. The extracted organic layer was washed with 29.4 g of water and 40.0 g of a saturated saline solution, and then, the organic layer was concentrated.
- The residue was purified by means of silica gel chromatography (SiO2; hexane/ethyl acetate = 1/1), to obtain 7.82 g (21.0 mmol) of the target 3-difluoromethyl-N-(7-fluoro-1,1,3-trimethyl-4-indanyl)-1-methyl-4-pyrazole carboxamide as a white crystal. The yield was 70.0%, and the purity was 94.4%. Melting point: 170.3°C
1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane) - δ value (ppm): 1.43 (3H,d), 1.38 (3H,s), 1.44 (3H,s), 1.66 (1H,dd), 2.21 (1H,dd), 3.38 (1H,m), 3.93 (3H,s), 6.81 (1s,bs), 6.95 (1H,t), 6.70 (1H,m), 7.81 (1H,bs), 8.03 (1H,bs)
- In the light of the above, it is noted that in the synthesis method according to the present invention, on the occasion of the reaction, it is not needed to remove the by-produced alcohol or phenol outside the reaction system, to allow the reaction to proceed while shifting the equilibrium toward the reaction production system as in Reference Example 1-1, and thus, the reaction can be completed without removing the by-produced alcohol or phenol outside the reaction system; and moreover, on the occasion of the treatment, such as isolation, after the reaction, an operation, such as extraction, is not needed, and the pyrazole-4-carboxamide derivative can be obtained in high yield and high purity by an extremely simple method in which after completion of the reaction, water is added, cooling is performed to deposit a crystal, and the crystal is subjected to solid-liquid separation.
- To 48.1 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 22.46 g (0.110 mol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 9.42 g (0.100 mol) of aniline were added in a nitrogen atmosphere.
- Subsequently, 13.61 g (0.20 mol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 81°C for 3 hours. The reaction mixture was cooled to 68°C, and then, 99.55 g of water was added, and cooling to 1.5°C was performed, whereby a crystal was deposited. The crystal was separated by means of filtration and washed with 99.62 g of water. The crystal after washing was dried. As a result, 24.26 g of 3-(difluoromethyl)-1-methyl-N-phenyl-4-pyrazole carboxamide was obtained as a white crystal. The yield was 95.5% (on a basis of aniline), and the purity was 99.9% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- Melting point: 108.7°C
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane)
- δ value (ppm): 3.92 (3H,s), 6.92 (1H,s), 7.14 (1H,t), 7.35 (2H,t), 7.59 (2H,d), 8.00 (1H,s), 8.17 (1H,s)
- To 50.3 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 23.36 g (0.114 mol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 11.13 g (0.104 mol) of 3-methylaniline were added in a nitrogen atmosphere.
- Subsequently, 14.14 g (0.208 mol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 80°C for 2 hours. The reaction mixture was cooled to 69°C, and then, 103.58 g of water was added, and cooling to 2°C was performed, whereby a crystal was deposited. The crystal was separated by means of filtration and washed with 77.97 g of water. The crystal after washing was dried. As a result, 25.57 g of 3-(difluoromethyl)-N-(3'-methylphenyl)-1-methyl-4-pyrazole carboxamide was obtained as a white crystal. The yield was 92.8% (on a basis of 3-methylaniline), and the purity was 99.7% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- Melting point: 110.8°C
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane)
- δ value (ppm): 2.36 (3H,s), 3.94 (3H,s), 6.90 (1H,t), 6.96 (1H,d), 7.24 (1H,t), 7.90 (1H,d), 7.44 (1H,s), 8.00 (1H,s), 8.08 (1H,bs)
- To 48.2 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 22.45 g (0.110 mol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 11.35 g (0.102 mol) of 3-fluoroaniline were added in a nitrogen atmosphere.
- Subsequently, 13.70 g (0.201 mol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 80°C for 2.5 hours. The reaction mixture was cooled to 67°C, and then, 100.29 g of water was added, and cooling to 2°C was performed, whereby a crystal was deposited. The crystal was separated by means of filtration and washed with 53.56 g of water. The crystal after washing was dried. As a result, 26.16 g of 3-(difluoromethyl)-1-methyl-N-(3'-fluorophenyl)-4-pyrazole carboxamide was obtained as a white crystal. The yield was 95.1% (on a basis of 3-fluoroaniline), and the purity was 99.9% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- Melting point: 120.7°C
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: DMSOd6, internal standard substance: tetramethylsilane)
- δ value (ppm): 3.96 (3H,s), 6.91 (1H,dt), 7.31 (1H,t), 7.34-7.43 (2H,m), 7.66 (1H,td), 8.48 (1H,s), 10.19 (1H,bs)
- To 48.3 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 22.47 g (0.110 mol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 13.77 g (0.102 mol) of 2,6-dimethylaniline were added in a nitrogen atmosphere.
- Subsequently, 13.66 g (0.201 mol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 80°C for 2 hours. The reaction mixture was cooled to 67°C, and then, 100.79 g of water was added, and cooling to 2°C was performed, whereby a crystal was deposited. The crystal was separated by means of filtration and washed with 59.60 g of water. The crystal after washing was dried. As a result, 18.32 g of 3-(difluoromethyl)-1-methyl-N-(2',6'-dimethylphenyl)-4-pyrazole carboxamide was obtained as a white crystal. The yield was 64.1% (on a basis of 2,6-dimethylaniline), and the purity was 99.7% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- Melting point: 158.6°C
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane)
- δ value (ppm): 2.27 (6H,s), 3.90 (3H,s), 6.90 (1H,t), 7.10-7.16 (3H,m), 7.74 (1H,bs), 7.97 (1H,s)
- To 38.6 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 17.97 g (0.088 mol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 13.78 g (0.081 mol) of 2-biphenylamine were added in a nitrogen atmosphere.
- Subsequently, 10.97 g (0.161 mol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 80°C for 2 hours. The reaction mixture was cooled to 69°C, and then, 78.81 g of water was added, and cooling to 2°C was performed, whereby a crystal was deposited. The crystal was separated by means of filtration and washed with 40.25 g of water. The crystal after washing was dried. As a result, 23.10 g of 3-(difluoromethyl)-1-methyl-N-(2-biphenyl)-4-pyrazole carboxamide was obtained as a white crystal. The yield was 86.7% (on a basis of 2-biphenylamine), and the purity was 96.7% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- Melting point: 127.4°C
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane)
- δ value (ppm): 3.88 (3H,s), 6.75 (1H,t), 7.20-7.29 (2H,m), 7.37-7.47 (6H,m), 7.70 (1H,s), 7.80 (1H,bs), 8.29 (1H,d)
- To 38.8 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 18.8 g (0.0921 mol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 21.72 g (0.085 mol) of 3',4'-dichloro-5-fluorobiphenyl-2-ylamine were added in a nitrogen atmosphere.
- The 3',4'-dichloro-5-fluorobiphenyl-2-ylamine was prepared by reference to
WO 2006/024388 A . - Subsequently, 11.56 g (0.170 mol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 80°C for 2 hours. The reaction mixture was cooled to 69°C, and then, 78.71 g of water was added, and cooling to 2°C was performed, whereby a crystal was deposited. The crystal was separated by means of filtration and washed with 40.30 g of water. The crystal after washing was dried. As a result, 33.10 g of 3-(difluoromethyl)-1-methyl-N-(3', 4'-dichloro-5-fluorobiphenyl-2-yl)-4-pyrazole carboxamide was obtained as a white crystal. The yield was 94.0% (on a basis of 3',4'-dichloro-5-fluorobiphenyl-2-ylamine), and the purity was 98.8% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- Melting point: 146.1°C
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane)
- δ value (ppm): 3.91 (3H,s), 6.67 (1H,t), 6.972 (1H,dd), 7.10-7.14 (1H,m), 7.20 (1H,dd), 7.47-7.51 (2H,m), 7.73 (1H,bs), 7.90 (1H,s), 8.09 (1H,dd)
- To 38.6 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 17.97 g (0.088 mol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 13.78 g (0.081 mol) of 3',4',5'-trifluorobiphenyl-2-ylamine were added in a nitrogen atmosphere.
- The 3',4',5'-trifluorobiphenyl-2-ylamine was prepared by reference to
WO 2010/094736 A . - Subsequently, 10.97 g (0.161 mol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 80°C for 2 hours. The reaction mixture was cooled to 69°C, and then, 78.90 g of water was added, and cooling to 2°C was performed, whereby a crystal was deposited. The crystal was separated by means of filtration and washed with 40.30 g of water. The crystal after washing was dried. As a result, 28.52 g of 3-(difluoromethyl)-1-methyl-N-(3',4',5'-trifluorobiphenyl-2-yl)-4-pyrazole carboxamide was obtained as a white crystal. The yield was 92.3% (on a basis of 3',4',5'-trifluorobiphenyl-2-ylamine), and the purity was 97.7% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- Melting point: 156.2°C
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane)
- δ value (ppm): 3.92 (3H,s), 6.64 (1H,t), 6.99-7.03 (2H,m), 7.20-7.25 (2H,m), 7.41-7.45 (1H,m), 7.81 (1H,bs), 7.96 (1H,s), 8.14 (1H,d)
- To 48.1 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 22.50 g (0.110 mol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 20.13 g (0.100 mol) of a mixture of N-[(1RS,4SR,9RS)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl]a mine and N-[(1RS,4SR,9SR)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yllamine were added in a nitrogen atmosphere.
- The mixture of N-[(1RS,4SR,9RS)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl]amine and N-[(1RS,4SR,9SR)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl]a mine was prepared by reference to
WO 2007/115765 A (PTL 4). - Subsequently, 13.61 g (0.200 mol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 81°C for 3 hours. The reaction mixture was cooled to 68°C, and then, 99.80 g of water was added, and cooling to 1.5°C was performed, whereby a crystal was deposited. The crystal was separated by means of filtration and washed with 100.00 g of water. The crystal after washing was dried. As a result, 33.07 g of a mixture of a 2-syn isomer: 3-(difluoromethyl)-1-methyl-N-[(1RS,4SR,9RS)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl]pyrazole-4-caboxamide and a 2-anti isomer: 3- (difluoromethyl)-1-methyl-N- [(1RS, 4SR,9SR)-1, 2, 3, 4-tetrahydro-9-isopropyl-1, 4-methanonaphthalen-5-yl]pyrazole-4-caboxamide was obtained as a white crystal. The yield was 92.0% (on a basis of the mixture of N-[(1RS,4SR,9RS)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl]amine and N-[(1RS,4SR,9SR)-1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl] amine), and the purity was 99.5% (the total sum of HPLC area percentages of the syn-form and the anti-form), and a purification operation, such as recrystallization, was not needed.
- Melting point: 130.0°C (syn-form) and 144.4°C (anti-form)
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane)
- δ value (ppm): syn-form: 0.8 (6H,s), 1.0 (1H,m), 1.2-2.0 (5H,m), 3.2-3.4 (2H,m), 4.0 (3H,s), 6.6-8.2 (6H,m), and anti-form: 0.9 (6H,s), 1.0-2.0 (6H,m), 3.2-3.4 (2H,m), 4.0 (3H,s), 6.7-8.1 (6H,m)
- To 13.0 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 6.09 g (0.030 mol) of ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 6.62 g (0.027 mol) of N-[(1RS,4SR)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yllamine were added in a nitrogen atmosphere.
- The N-[(1RS,4SR)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]amine was prepared by reference to
WO 2010/049228 A . - Subsequently, 3.70 g (0.054 mol) of sodium ethoxide was added at an internal temperature of 7.0°C, the temperature was raised to an internal temperature of 65°C over 2 hours, and the contents were stirred at the same temperature for 8 hours. The reaction mixture was cooled to 63°C, and then, 26.87 g of water was added, and cooling to 4.4°C was performed, whereby a crystal was deposited. The crystal was separated by means of filtration and washed with 152.60 g of water. The crystal after washing was dried. As a result, 10.31 g of 3-(difluoromethyl)-1-methyl-N-[(1RS,4SR)-9-(dichloromethylene)-1,2,3,4-tetrahyd ro-1,4-methanonaphthalen-5-yl]pyrazole-4-carboxamide was obtained as a white crystal. The yield was 95.8% (on a basis of N-[(1RS,4SR)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5 -yl]amine), and the purity was 98.4% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- Melting point: 147.4°C
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane)
- δ value (ppm): 1.38 (1H,m), 1.49 (1H,m), 2.10 (2H,m), 3.95 (3H,s, overlapped by 1H,m), 4.06 (1H,m), 6.89 (1H,t, J = 54Hz), 7.03 (1H,d), 7.17 (1H,t), 7.82 (1H,d), 8.06 (1H,s), 8.11 (1H,bs)
- To 17.9 mL of N-methylpyrrolidone in a 300-mL four-necked flask, 24.56 g (0.111 mol) of ethyl 3-(trifluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate and 18.43 g (0.101 mol) of (RS)-N-[2-(1,3-dimethylbutyl)-3-thienyl]amine were added in a nitrogen atmosphere.
- The (RS)-N-[2-(1,3-dimethylbutyl)-3-thienyl]amine was prepared by reference to
EP 0737682 A (PTL 6). - Subsequently, 13.65 g (0.201 mol) of sodium ethoxide was added, and the contents were stirred at an internal temperature of 70°C for 7 hours. To the reaction mixture, 48.30 g of water was added at the same temperature, and after stirring for 30 minutes, the resultant was allowed to stand at 65°C, to separate the aqueous layer. The organic layer was naturally cooled to 12.0°C over 12 hours while stirring. Subsequently, 49.58 g of water was added to the organic layer, followed by stirring at 30°C for 30 minutes. As a result, a crystal was gradually deposited. After stirring at the same temperature for 4 hours, the crystal was separated by means of filtration and washed with 77.60 g of water. The crystal after washing was dried. As a result, 33.44 g of (RS)-N-[2-(1,3-dimethylbutyl)-3-thienyl]-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide was obtained as a white crystal. The yield was 93.2% (on a basis of (RS)-N-[2-(1,3-dimethylbutyl)-3-thienyl]amine), and the purity was 99.8% (HPLC area percentage), and a purification operation, such as recrystallization, was not needed.
- Melting point: 108.5°C
- 1H-NMR (1H resonance frequency: 500 MHz, measurement solvent: CDCl3, internal standard substance: tetramethylsilane)
- δ value (ppm): 0.86 (6H,d), 1.25 (3H,d), 1.4-1.7 (3H,m), 3.09 (1H,m), 3.94 (3H,s), 7.11 (1H,d), 7.39 (1H,s), 7.61 (1H,bs), 8.02 (1H,s)
- In the light of the above, different from the present invention, the background art is in general concerned with the usual aminolysis reaction in which a by-produced alcohol or phenol is removed outside the reaction system through fractionation or the like, and the equilibrium is shifted toward the reaction production system, thereby completing the reaction, and it may be said that the treatment after the reaction is also usual one. On the other hand, the present invention is concerned with a technology in which the pyrazole-4-caroxamide derivative can be obtained in high yield and high purity by a simple method in which the reaction can be completed without removing the by-produced alcohol or phenol outside the system, and as for the treatment after the reaction, water is added after the end of the reaction, to deposit a crystal, and thus, it is noted that the present invention is concerned with an extremely simple and safe method.
- The production method of the present invention is useful as an industrial production method in which the pyrazole-4-carboxamide derivative that is useful as an agricultural fungicide can be obtained in high yield and high purity through a short process and a simple operation.
Claims (8)
- A method of producing a pyrazole-4-carboxamide derivative represented by the formula (1):R1 is a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group,R2 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group,R3 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, andin Q1, R4, R5, and R6 are the same as or different from each other and are each a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, or a C3-C6 halocycloalkyl group, provided that R5 and R6 may be bonded to each other to form a C3-C6 cycloalkyl group,V represents CH(R7), N(R8), an oxygen atom, or a sulfur atom, and R7 and R8 are each a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, or a C3-C6 halocycloalkyl group,Y represents a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, an SH group, a C1-C4 alkylthio group, or a C1-C4 haloalkylthio group, andm is an integer of 0 to 3;in Q2, Y1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, andn is an integer of 1 to 5, and when n is 2, 3, 4, or 5, then Y1's may be the same as or different from each other;in Q3, Y1 and Z each represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group,p represents an integer of 1 to 4, and when p is 2, 3, or 4, then Y1's may be the same as or different from each other, andn represents an integer of 1 to 5, and when n is 2, 3, 4, or 5, then Z's may be the same as or different from each other;in Q4, R9, R10, R11, R12, R13, and R14 are the same as or different from each other and each represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, R11 and R12 may be bonded to each other to form a C3-C6 cycloalkyl group and R13 and R14 may be bonded to each other to form a C3-C6 cycloalkyl group, andW represents a methylene group, a methine group substituted with a C1-C6 haloalkyl group, or a terminal end-substituted vinyl group represented by the formula (4):wherein T represents a C1-C6 haloalkyl group or a halogen atom;in Q5, Y1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group,m represents an integer of 1 to 3, and when m is 2 or 3, then Y1's may be the same as or different from each other, andG represents an oxygen atom, a sulfur atom, or N(R15), and R15 represents a hydrogen atom or a C1-C6 alkyl group; andin Q6, Y1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group,m represents an integer of 1 to 3, and when m is 2 or 3, then Y1's may be the same as or different from each other, andG represents an oxygen atom, a sulfur atom, or N(R15), and R15 represents a hydrogen atom or a C1-C6 alkyl group,wherein,R1 is a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group,R2 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group,R3 is a hydrogen atom, a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, an aralkyl group, or an aryl group, andR is a C1-C4 alkyl group or an optionally substituted phenyl group,and an amine represented by the formula (3):
H2N-Qx (3)
whereinin Q1, R4, R5, and R6 are the same as or different from each other and are each a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, or a C3-C6 halocycloalkyl group, provided that R5 and R6 may be bonded to each other to form a C3-C6 cycloalkyl group,V represents CH(R7), N(R8), an oxygen atom, or a sulfur atom, and R7 and R8 are each a hydrogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C6 cycloalkyl group, or a C3-C6 halocycloalkyl group,Y represents a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkoxy group, a C1-C4 haloalkoxy group, an SH group, a C1-C4 alkylthio group, or a C1-C4 haloalkylthio group, andm is an integer of 0 to 3;in Q2, Y1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, andn is an integer of 1 to 5, and when n is 2, 3, 4, or 5, then Y's may be the same as or different from each other;in Q3, Y1 and Z each represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group,p represents an integer of 1 to 4, and when p is 2, 3, or 4, then Y's may be the same as or different from each other, andn represents an integer of 1 to 5, and when n is 2, 3, 4, or 5, then Z's may be the same as or different from each other;in Q4, R9, R10, R11, R12, R13, and R14 are the same as or different from each other and each represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group, R11 and R12 may be bonded to each other to form a C3-C6 cycloalkyl group, and R13 and R14 may be bonded to each other to form a C3-C6 cycloalkyl group, andW represents a methylene group, a methine group substituted with a C1-C6 haloalkyl group, or a terminal end-substituted vinyl group represented by the formula (4):wherein T represents a C1-C6 haloalkyl group or a halogen atom;in Q5, Y1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group,m represents an integer of 1 to 3, and when m is 2 or 3, then Y1's may be the same as or different from each other, andG represents an oxygen atom, a sulfur atom, or N(R15), and R15 represents a hydrogen atom or a C1-C6 alkyl group; andin Q6, Y1 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, an SH group, a C1-C6 alkylthio group, or a C1-C6 haloalkylthio group,m represents an integer of 1 to 3, and when m is 2 or 3, then Y1's may be the same as or different from each other, andG represents an oxygen atom, a sulfur atom, or N(R15), and R15 represents a hydrogen atom or a C1-C6 alkyl group,
to an aminolysis reaction in a solvent in the presence of a base, provided that the reaction is completed without removing a by-produced alcohol or phenol,wherein the solvent to be used for the reaction is an aprotic solvent,the method further comprising:(i) after completion of the reaction, adding water to the reaction mixture to deposit the target material, and subjecting the resultant to filtration, followed by drying, to thereby obtain a pyrazole-4-carboxamide derivative, or(ii) after completion of the reaction, adding water to the reaction mixture, separating the aqueous layer to remove an unnecessary material from the organic layer containing the target material, adding water to the remaining organic layer to deposit the target material, and subjecting the resultant to filtration, followed by drying, to thereby obtain a pyrazole-4-carboxamide derivative. - The production method according to claim 1, wherein the base to be used for the reaction is a metal alkoxide.
- The production method according to claim 2, wherein the metal alkoxide is at least one selected from lithium methoxide, lithium ethoxide, sodium methoxide, sodium ethoxide, potassium methoxide, and potassium ethoxide.
- The production method according to any one of claims 1 to 3, wherein, as for a charging ratio of the pyrazole carboxylic acid ester represented by the formula (2) and the amine represented by the formula (3), the amount of the pyrazole carboxylic acid ester is in a range of 1.0 to 2.0 equivalents to 1.0 equivalent of the amine.
- The production method according to any one of claims 1 to 4, wherein the use amount of the base is in a range of 1.0 to 7.0 equivalents to 1.0 equivalent of the amine represented by the formula (3).
- The production method according to any one of claims 1 to 5, wherein the solvent to be used for the reaction is selected from the group consisting of N,N-dimethylacetamide, N-methylpyrrolidone, N,N-dimethylformamide and dimethyl sulfoxide.
- The production method according to any one of claims 1 to 6, wherein the use amount of the solvent is in a range of 0.5 to 10.0 equivalents relative to the amine represented by the formula (3).
- The production method according to any one of claims 1 to 7, wherein the amount of water needed for deposition in the above (i) and (ii) is about 1.0 to 7.0 in terms of a mass ratio relative to the used solvent.
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EP1904450A1 (en) | 2005-07-18 | 2008-04-02 | Syngeta Participations AG | Pyrazole-4- carboxamide derivatives as microbiocides |
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